ENST00000683572.1:n.617A>C
|
|
|
ENST00000341947.7:c.4811A>C
MANE Select
|
ENSP00000339915.2:p.Asn1604Thr
|
|
ENST00000341947.6:c.4811A>C
|
ENSP00000339915.2:p.Asn1604Thr
|
|
ENST00000361917.5:c.4490A>C
|
ENSP00000355123.1:p.Asn1497Thr
|
|
ENST00000374708.8:c.4553A>C
|
ENSP00000363840.4:p.Asn1518Thr
|
|
ENST00000477772.1:n.601A>C
|
|
|
NM_080679.2:c.4490A>C
|
NP_542410.2:p.Asn1497Thr
|
|
NM_080680.2:c.4811A>C
|
NP_542411.2:p.Asn1604Thr
|
|
NM_080681.2:c.4553A>C
|
NP_542412.2:p.Asn1518Thr
|
|
XM_011514298.1:c.3965A>C
|
XP_011512600.1:p.Asn1322Thr
|
|
XM_011514299.1:c.4097A>C
|
XP_011512601.1:p.Asn1366Thr
|
|
XM_011514300.1:c.3917A>C
|
XP_011512602.1:p.Asn1306Thr
|
|
XM_011514301.1:c.3854A>C
|
XP_011512603.1:p.Asn1285Thr
|
|
XM_011514302.1:c.3698A>C
|
XP_011512604.1:p.Asn1233Thr
|
|
XM_011514299.2:c.4097A>C
|
XP_011512601.1:p.Asn1366Thr
|
|
XM_011514300.2:c.3917A>C
|
XP_011512602.1:p.Asn1306Thr
|
|
XM_011514302.2:c.3698A>C
|
XP_011512604.1:p.Asn1233Thr
|
|
XM_017010250.1:c.4811A>C
|
XP_016865739.1:p.Asn1604Thr
|
|
XM_017010251.2:c.3629A>C
|
XP_016865740.1:p.Asn1210Thr
|
|
NM_080680.3:c.4811A>C
MANE Select
|
NP_542411.2:p.Asn1604Thr
|
|
NM_080681.3:c.4553A>C
|
NP_542412.2:p.Asn1518Thr
|
|
NM_080679.3:c.4490A>C
|
NP_542410.2:p.Asn1497Thr
|
|